Obesity and Antibiotic Tissue Concentration

NCT00980486 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 31

Last updated 2010-10-08

No results posted yet for this study

Summary

The purpose of this study is to determine whether the dose of prophylactic antibiotics at the time of cesarean delivery requires adjustment in obese and overweight patients in order to achieve optimal antimicrobial activity.

Conditions

Sponsors & Collaborators

  • University of California, Irvine

    collaborator OTHER
  • MemorialCare

    lead OTHER

Principal Investigators

  • Kenneth Chan, MD · Long Beach Memorial Medical Center

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2010-06-30
Completion
2010-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00980486 on ClinicalTrials.gov